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Noam Shomron
Researcher at Tel Aviv University
Publications - 244
Citations - 8929
Noam Shomron is an academic researcher from Tel Aviv University. The author has contributed to research in topics: microRNA & Gene. The author has an hindex of 49, co-authored 212 publications receiving 7442 citations. Previous affiliations of Noam Shomron include International Computer Science Institute & Massachusetts Institute of Technology.
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Intensified vmPFC surveillance over PTSS under perturbed microRNA-608/AChE interaction.
Tamar Lin,Alon Simchovitz,Shani Shenhar-Tsarfaty,S. Vaisvaser,Roee Admon,Geula Hanin,Mor Hanan,Efrat Kliper,Yair Bar-Haim,Noam Shomron,Guillén Fernández,Gadi Lubin,Eyal Fruchter,Talma Hendler,Hermona Soreq +14 more
TL;DR: Co-intensified amygdala and ventromedial prefrontal cortex emotional responses that may overcome PTSS in individuals with the single-nucleotide polymorphism (SNP) rs17228616 in the acetylcholinesterase (AChE) gene are reported.
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Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration
Eran Pras,Dana Kristal,Nadav Shoshany,Dina Volodarsky,Inna Vulih,Gershon Celniker,Ofer Isakov,Noam Shomron,Elon Pras,Elon Pras +9 more
TL;DR: A null-variant in HMCN1 has been identified in one AMD family, and a missense variant in CFI was discovered in two other families, which confirm the genetic complexity and significance of rare genetic variants in the pathogenesis of AMD.
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Evaluation of optimization techniques for variable selection in logistic regression applied to diagnosis of myocardial infarction.
TL;DR: A large dataset is used to predict the diagnosis of myocardial infarction in patients reporting to an emergency room with chest pain and it is indicated that some of the examined methods are well suited for variable selection in logistic regression.
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Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.
Alicia Guemez-Gamboa,Ahmet Okay Caglayan,Valentina Stanley,Anne Gregor,Maha S. Zaki,Sahar N. Saleem,Damir Musaev,Jennifer McEvoy-Venneri,Denice Belandres,Naiara Akizu,Jennifer L. Silhavy,Jana Schroth,Rasim Ozgur Rosti,Brett Copeland,Steven M. Lewis,Rebecca Fang,Mahmoud Y. Issa,Hüseyin Per,Hakan Gümüş,Ayşe Kaçar Bayram,Sefer Kumandaş,Gozde Tugce Akgumus,Emine Z. Erson-Omay,Katsuhito Yasuno,Kaya Bilguvar,Gali Heimer,Nir Pillar,Noam Shomron,Daphna Weissglas-Volkov,Yuval Porat,Yaron Einhorn,Stacey Gabriel,Bruria Ben-Zeev,Murat Gunel,Joseph G. Gleeson,Joseph G. Gleeson +35 more
TL;DR: To identify causes of the autosomal‐recessive malformation, diencephalic‐mesencephalic junction dysplasia (DMJD) syndrome, researchers use a probabilistic approach to evaluate the immune defences of the central nervous system.
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Regulation of Complement-Dependent Cytotoxicity by MicroRNAs miR-200b, miR-200c, and miR-217.
TL;DR: Overall, the data demonstrate miRNA regulation of cell sensitivity to CDC, and identified miR-200b, mi-200c, and mi-217 as regulators of mortalin and, perhaps indirectly, of CD46 and CD55.